摘要
该文以2,4-二羟基苯乙酮和3,4-二羟基苯甲醛为原料,经C-香叶基化或C-异戊烯基化、硫酸二甲酯保护、羟醛缩合得到最终产物。合成的关键是将香叶基或异戊烯基选择性引入2,4-二羟基苯乙酮的3位。所有化合物的结构都经过1 H-NMR,13 C-NMR,IR,MS分析标准。
The final products were accomplished from 2,4-dihydroxy acetophenone and 3,4-dihydroxy benzaldehyde,by C-geranylation or C-prenylation,methylation,condensation and cyclization.The key step was pentenyl or geranyl selective introduced into 2,4-dihydroxyacetophenone.All structures of compounds were confirmed by 1 H NMR,13 C NMR,IR and MS.
出处
《广西师范学院学报(自然科学版)》
2016年第1期47-51,共5页
Journal of Guangxi Teachers Education University(Natural Science Edition)
基金
广西自然科学基金2013GXNSFAAO19041
广西研究生教育创新计划项目(20121106030703M02
20120603R03)
西南民族药协同创新中心资助课题(CICSEM2013-B6)